WO2019078688A2 - 리튬 이차전지용 양극 활물질, 이의 제조방법, 이를 포함하는 리튬 이차전지용 양극 및 리튬 이차전지 - Google Patents

리튬 이차전지용 양극 활물질, 이의 제조방법, 이를 포함하는 리튬 이차전지용 양극 및 리튬 이차전지 Download PDF

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WO2019078688A2
WO2019078688A2 PCT/KR2018/012452 KR2018012452W WO2019078688A2 WO 2019078688 A2 WO2019078688 A2 WO 2019078688A2 KR 2018012452 W KR2018012452 W KR 2018012452W WO 2019078688 A2 WO2019078688 A2 WO 2019078688A2
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lithium
transition metal
active material
positive electrode
secondary battery
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PCT/KR2018/012452
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French (fr)
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WO2019078688A3 (ko
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주서희
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주식회사 엘지화학
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Priority to CN201880066202.2A priority Critical patent/CN111201647B/zh
Priority to JP2020518406A priority patent/JP7009015B2/ja
Priority to US16/754,027 priority patent/US11489156B2/en
Publication of WO2019078688A2 publication Critical patent/WO2019078688A2/ko
Publication of WO2019078688A3 publication Critical patent/WO2019078688A3/ko

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    • C01G53/00—Compounds of nickel
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    • C01G53/40—Nickelates
    • C01G53/42—Nickelates containing alkali metals, e.g. LiNiO2
    • C01G53/44—Nickelates containing alkali metals, e.g. LiNiO2 containing manganese
    • C01G53/50—Nickelates containing alkali metals, e.g. LiNiO2 containing manganese of the type [MnO2]n-, e.g. Li(NixMn1-x)O2, Li(MyNixMn1-x-y)O2
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    • H01M10/052—Li-accumulators
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    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
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    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/485—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
    • H—ELECTRICITY
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    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
    • H01M4/505—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
    • H—ELECTRICITY
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    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
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    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
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    • H01M4/00—Electrodes
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    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/5825—Oxygenated metallic salts or polyanionic structures, e.g. borates, phosphates, silicates, olivines
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    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • C—CHEMISTRY; METALLURGY
    • C01—INORGANIC CHEMISTRY
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    • C01P2006/40—Electric properties
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    • C01—INORGANIC CHEMISTRY
    • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00—Physical properties of inorganic compounds
    • C01P2006/80—Compositional purity
    • H—ELECTRICITY
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    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
    • H01M2004/028—Positive electrodes
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Definitions

  • the present invention relates to a positive electrode active material for a lithium secondary battery, a method for producing the positive electrode active material, a positive electrode for a lithium secondary battery including the positive electrode active material, and a lithium secondary battery.
  • lithium secondary batteries having a high energy density and voltage, a long cycle life, and a low self-discharge rate are commercially available and widely used.
  • Lithium transition metal complex oxides are used as the positive electrode active material of lithium secondary batteries, and lithium cobalt composite metal oxides such as LiCoO 2 having a high operating voltage and excellent capacity characteristics are mainly used.
  • LiCoO 2 has very poor thermal properties due to the destabilization of the crystal structure due to the depolymerization.
  • LiCoO 2 is expensive, it can not be used in large quantities as a power source for fields such as electric vehicles and the like.
  • Lithium manganese composite metal oxides such as LiMnO 2 or LiMn 2 O 4
  • lithium iron phosphate compounds such as LiFePO 4
  • lithium nickel composite metal oxides such as LiNiO 2
  • LiNiO 2 has a lower thermal stability than LiCoO 2
  • a lithium nickel cobalt metal oxide in which a part of Ni is substituted with Co and Mn or Al has been developed as a method for improving low thermal stability while maintaining excellent reversible capacity of LiNiO 2 .
  • cathode active material which can contain a lithium-nickel-cobalt metal oxide, wherein a uniform coating layer is formed on the surface of the lithium nickel-cobalt metal oxide to reduce the resistance and improve the stability and lifetime have.
  • a first technical object of the present invention is to provide a lithium-transition metal oxide coated with a lithium-containing inorganic compound on the surface of an M 1 , M 2 -doped lithium transition metal oxide, .
  • a second object of the present invention is to provide a method for producing a cathode active material capable of uniformly forming a lithium-containing inorganic compound layer on the surface of an M 1 , M 2 -doped lithium transition metal oxide by using a wet process.
  • a third object of the present invention is to provide a positive electrode for a lithium secondary battery comprising the positive electrode active material.
  • a fourth aspect of the present invention is to provide a lithium secondary battery including the positive electrode for a lithium secondary battery.
  • the present invention relates to a lithium transition metal oxide represented by the following general formula (1); And a lithium-containing inorganic compound layer formed on the surface of the lithium transition metal oxide.
  • X is at least one or more selected from the group consisting of Mn and Al
  • M 1 is at least one or more selected from the group consisting of S, F, P, and N
  • M 2 is at least one selected from the group consisting of Zr, B
  • the present invention also provides a method for preparing a lithium transition metal oxide represented by Formula 1 by mixing and firing a doping element M 1 -doped transition metal hydroxide precursor, a lithium source material, and a doping element M 2 -containing raw material, Mixing the inorganic acid aqueous solution with the lithium transition metal oxide to prepare a mixed solution; And drying and heat-treating the mixed solution to form a lithium-containing inorganic compound layer on the surface of the lithium transition metal oxide.
  • a method for preparing a lithium transition metal oxide represented by Formula 1 by mixing and firing a doping element M 1 -doped transition metal hydroxide precursor, a lithium source material, and a doping element M 2 -containing raw material, Mixing the inorganic acid aqueous solution with the lithium transition metal oxide to prepare a mixed solution; And drying and heat-treating the mixed solution to form a lithium-containing inorganic compound layer on the surface of the lithium transition metal oxide.
  • a positive electrode for a lithium secondary battery comprising the positive electrode active material according to the present invention.
  • a lithium secondary battery comprising a positive electrode according to the present invention.
  • the structural stability of the lithium transition metal oxide can be improved, and the lifetime characteristics can be improved accordingly.
  • the lithium-containing inorganic compound layer on the surface of the lithium transition metal oxide, the lithium ion mobility can be improved and the charge / discharge efficiency can be improved, and the cathode active material with reduced resistance can be produced. Further, it is possible to manufacture a battery having improved lifetime characteristics as the structural stability and surface stability of the positive electrode active material are improved.
  • the lithium-containing inorganic compound layer can be uniformly coated on the surface of the lithium transition metal oxide by preparing the cathode active material using a wet process of mixing the lithium transition metal oxide with the inorganic acid.
  • the lithium impurity existing on the surface of the lithium transition metal oxide reacts with the inorganic acid to form the lithium-containing inorganic compound layer, the amount of lithium impurity on the surface of the finally produced positive electrode active material can be reduced. Accordingly, expansion of the battery due to side reaction between the positive electrode active material and the electrolyte can be prevented beforehand, and the electrochemical performance of the secondary battery can be further improved.
  • FIG. 1 is a graph showing lifetime maintenance ratios and resistance increase rates of the lithium secondary batteries manufactured in Example 1 and Comparative Example 1 according to cycles.
  • FIG. 1 is a graph showing lifetime maintenance ratios and resistance increase rates of the lithium secondary batteries manufactured in Example 1 and Comparative Example 1 according to cycles.
  • lithium transition metal oxides have a problem in that the interfacial resistance between the electrode and the electrolyte is increased as the charge and discharge are repeated, and the stability and lifetime characteristics of the battery such as decomposition of the electrolyte drastically deteriorate.
  • a lithium-containing inorganic compound layer is coated on the surface of the lithium transition metal oxide using a dry process.
  • the dry coating method is used, the lithium-containing inorganic compound layer is not uniformly coated, and thus the stability of the cathode active material is not improved.
  • the present inventors not only improved the structural stability of the cathode active material by coating the lithium transition metal oxide with at least two doping elements, but also formed the lithium-containing inorganic compound layer on the surface of the lithium transition metal oxide, . Further, in the production of the lithium-containing inorganic compound layer, by using the wet process of mixing the lithium transition metal oxide with the inorganic acid aqueous solution, the amount of lithium impurity present on the surface can be reduced while uniformly coating the lithium- A battery having improved stability and lifespan characteristics can be produced, and the present invention has been completed.
  • the positive electrode active material according to the present invention comprises a lithium-transition metal oxide represented by the following formula (1) and a lithium-containing inorganic compound layer formed on the surface of the lithium-transition metal oxide:
  • X is at least one or more selected from the group consisting of Mn and Al
  • M 1 is at least one or more selected from the group consisting of S, F, P, and N
  • M 2 is at least one selected from the group consisting of Zr, B
  • the cathode active material may include a lithium transition metal oxide containing at least 60 mol%, preferably 60 mol% to 99 mol% nickel relative to the total molar amount of the transition metal except lithium.
  • a lithium transition metal oxide containing at least 60 mol%, preferably 60 mol% to 99 mol% nickel relative to the total molar amount of the transition metal except lithium.
  • the lithium transition metal oxide may include a doping element M 1 and an M 2 -doped lithium transition metal oxide.
  • the lithium transition metal oxide is doped with at least two metal elements, M 1 and M 2 , the surface stability and structure stability depending on the positional difference of the doping material due to the difference in the diffusion rates of two different doping materials And the lifetime characteristics of the battery can be improved.
  • the lithium transition metal oxide contains only one of M 1 and M 2 as the doping element, the lifetime characteristics may be relatively degraded as compared with the case where the lithium transition metal oxide includes two kinds of doping elements.
  • the cathode active material may include 0.0001 to 5 parts by weight, preferably 0.001 to 0.01 part by weight, of the doping element M 1 relative to 100 parts by weight of the cathode active material.
  • the doping element M 1 may be at least one or more selected from the group consisting of S, F, P and N, and most preferably S.
  • the lithium transition metal oxide includes the doping element M 1 , the lifetime characteristics can be improved by securing the surface stability.
  • the cathode active material may include 0.0001 to 5 parts by weight, preferably 0.001 to 0.01 part by weight, of the doping element M 2 relative to 100 parts by weight of the cathode active material.
  • the doping element M 2 is at least one or more selected from the group consisting of Zr, B, Co, W, Mg, Ce, Ta, Ti, Sr, Ba, Hf, F, P, And preferably Zr.
  • the lithium transition metal oxide includes the doping element M 2 , thereby improving the structural stability of the lithium transition metal oxide and improving lifetime characteristics.
  • the lithium transition metal oxide is Li x Ni 0.8 Co 0.1 Mn 0.1 Zr 0.04 S 0.03 O 2 (1.0 x 1.10), Li x Ni 0 . 6 Co 0 . 2 Mn 0 . 2 Zr 0 . 05 S 0 . 03 O 2 (1.0? X? 1.10), Li x Ni 0 . 87 Co 0 . 07 Mn 0 . 06 Zr 0 . 03 S 0 . 03 O 2 (1.0? X? 1.10), Li x Ni 0 . 9 Co 0 . 05 Mn 0 . 05 Zr 0 . 03 S 0 . 03 O 2 (1.0? X? 1.10), Li x Ni 0 .
  • the cathode active material may include a lithium-containing inorganic compound layer formed on the surface of the lithium transition metal oxide.
  • the lithium-containing inorganic compound layer may be at least one selected from the group consisting of Li 3 BO 3 , LiBO 2 , Li 3 PO 4 , and LiPO 3 .
  • the inorganic compound layer containing lithium is formed on the surface of the lithium transition metal oxide, the mobility of the lithium ion can be improved, thereby improving the electric conductivity of the cathode active material and improving the charging / discharging efficiency of the battery. .
  • the lithium-containing inorganic compound layer may be uniformly formed on the entire surface of the surface of the lithium-transition metal oxide.
  • the lithium-containing inorganic compound may be formed to a thickness of 1 nm to 200 nm, preferably 3 nm to 100 nm.
  • the amount of the lithium impurity on the surface of the positive electrode active material is 0.1% by weight to 1.0% by weight, preferably 0.4% by weight to 0.8% by weight based on the total weight of the positive electrode active material.
  • the lithium impurity may be at least one selected from the group consisting of LiOH and Li 2 CO 3 .
  • the side reaction with the electrolyte during charging and discharging of the secondary battery can be reduced. Accordingly, expansion of the battery, which may occur due to side reactions between the lithium impurity existing on the surface of the positive electrode active material and the electrolyte solution, can be suppressed, and the structural stability and lifetime characteristics of the battery can be improved.
  • the amount of lithium impurity on the surface of the positive electrode active material may be measured by titrating with 0.1 M HCl using an acid-base titrator.
  • the kind and concentration of the acid used for the titration, the reference pH, and the like can be appropriately changed as needed.
  • the present invention also relates to a process for preparing M 1 and M 2 -doped lithium transition metal oxides by mixing and firing a doping element M 1 -doped transition metal hydroxide precursor, a lithium source material, and a doping element M 2 -containing raw material step; Mixing the inorganic acid aqueous solution with the lithium transition metal oxide to prepare a mixed solution; And drying and heat-treating the mixed solution to form a lithium-containing inorganic compound layer on the surface of the lithium transition metal oxide.
  • the doping element M 1 -doped transition metal hydroxide precursor, the lithium source material, and the doping element M 2 -containing source material are mixed and fired to produce M 1 and M 2 -doped lithium transition metal oxides.
  • the transition metal hydroxide precursor may have a nickel content of 60 mol% or more based on the total moles of the transition metal, and Ni b1 Co c1 X d1 M 1 e1 (OH) 2 (Wherein X is at least one or more selected from the group consisting of Mn and Al, M 1 is at least one or more selected from the group consisting of S, F, P and N, and 0.6? B1? 1.0, ? 0.2, 0? D1? 0.2, 0 ⁇ e1? 0.1).
  • the transition metal hydroxide precursor is selected from the group consisting of Ni 0.6 Co 0.2 Mn 0.2 S 0.03 (OH) 2 , Ni 0 . 8 Co 0 . 1 Mn 0 .
  • NiS 0.03 (OH) can be at least one selected from the group consisting of 2.
  • the content of nickel is 60 mol% or more with respect to the total number of moles of the transition metal hydroxide precursor, the capacity of the battery during the production of the battery can be increased.
  • the M 1 -doped transition metal hydroxide precursor can be used without particular limitation as long as it is a method of doping the doping element in the production of the transition metal hydroxide precursor.
  • the transition metal hydroxide precursor may be doped by coprecipitation reaction of the transition metal source materials included in the transition metal hydroxide precursor with the doping element M & lt ; 1 & gt ; -containing source material, or the transition metal hydroxide precursor produced by the coprecipitation reaction and the doping element M 1 wherein M 1 by mixing a raw material containing a dry heat treatment, and can be prepared the doped transition metal hydroxide precursor.
  • the lithium-source material is not particularly limited as long as it is a compound containing a lithium source, but lithium carbonate (Li 2 CO 3 ), lithium hydroxide (LiOH), LiNO 3 , CH 3 COOLi and Li 2 COO) 2 may be used.
  • the doping element M 1 -containing raw material may be a metal-containing oxide or hydroxide including at least one selected from the group consisting of S, F, P, and N, and the like.
  • the doping element M 2 -containing raw material is at least one selected from the group consisting of Zr, B, Co, W, Mg, Ce, Ta, Ti, Sr, Ba, Hf, F, P, Containing oxides or hydroxides and the like may be used.
  • the doping element M 1 -doped transition metal hydroxide precursor lithium source material: the doping element M 2 -containing source material has a molar ratio of 1: (1.00-1.30) :( 0-0.1), preferably 1: 1.10): (0.02 to 0.07).
  • the doping element M 1 -doped transition metal hydroxide precursor, the lithium source material, and the doping element M 2 -containing source material are mixed at the molar ratio within the above range, a lithium transition metal having excellent structural stability and excellent capacity characteristics Oxides can be produced.
  • the mixed solution through the mixing step is fired to prepare M 1 and M 2 -doped lithium transition metal oxides.
  • the firing may be performed at 700 ° C to 900 ° C, more preferably at 750 ° C to 850 ° C for 10 hours to 24 hours.
  • the firing temperature satisfies the above range, the cathode active material having the structural stability can be formed.
  • the M 1 and M 2 -doped lithium transition metal oxides prepared as described above may more preferably be represented by the following formula 1:
  • X is at least one or more selected from the group consisting of Mn and Al
  • M 1 is at least one or more selected from the group consisting of S, F, P, and N
  • M 2 is at least one selected from the group consisting of Zr, B
  • the lithium transition metal oxide is mixed with an inorganic acid aqueous solution to prepare a mixed solution.
  • the inorganic acid aqueous solution may be, for example, having a pH of 2 to 10, more preferably a pH of 4 to 7.
  • the inorganic acid aqueous solution may include at least one selected from the group consisting of boric acid (H 3 BO 3 ) and phosphoric acid (P 2 O 5 , H 3 PO 4 ).
  • the lithium-transition metal oxide may be mixed with the inorganic acid aqueous solution to cause an acid-base reaction between the lithium impurity present on the surface of the lithium-transition metal oxide and the inorganic acid aqueous solution, A lithium-containing inorganic compound may be formed.
  • the lithium impurity may be at least one selected from the group consisting of LiOH and Li 2 CO 3 , and the lithium impurity amount present on the surface of the lithium transition metal oxide is increased as the content of nickel contained in the lithium transition metal oxide is higher Or may be increased as the firing temperature is higher in the synthesis of the lithium transition metal oxide.
  • the lithium-containing inorganic compound may be produced by the following reaction.
  • the mixed solution is dried and heat-treated at 200 ° C to 400 ° C, preferably 250 ° C to 350 ° C to form a lithium-containing inorganic compound layer on the surface of the lithium-transition metal oxide.
  • the drying of the mixed solution is not particularly limited as long as it is a conventional method in the art, and may be performed by hot air drying, oven drying, vacuum drying, or the like.
  • the resulting lithium-containing inorganic compound layer has a thickness of 3 nm to 20 nm and can be uniformly formed over the entire surface of the lithium transition metal oxide.
  • the cathode for a secondary battery includes a cathode current collector, a cathode active material layer formed on the cathode current collector, and the cathode active material layer includes the cathode active material according to the present invention.
  • cathode active material is the same as that described above, a detailed description thereof will be omitted and only the remaining constitution will be specifically described below.
  • the positive electrode current collector is not particularly limited as long as it has conductivity without causing chemical changes in the battery.
  • carbon, nickel, titanium, , Silver or the like may be used.
  • the cathode current collector may have a thickness of 3 to 500 ⁇ , and fine unevenness may be formed on the surface of the current collector to increase the adhesive force of the cathode active material.
  • it can be used in various forms such as a film, a sheet, a foil, a net, a porous body, a foam, and a nonwoven fabric.
  • the cathode active material layer may include a conductive material and, optionally, a binder optionally together with the cathode active material.
  • the cathode active material may be contained in an amount of 80 to 99% by weight, more specifically 85 to 98.5% by weight based on the total weight of the cathode active material layer. When included in the above content range, excellent capacity characteristics can be exhibited.
  • the conductive material is used for imparting conductivity to the electrode.
  • the conductive material is not particularly limited as long as it has electron conductivity without causing chemical change. Specific examples thereof include graphite such as natural graphite and artificial graphite; Carbon-based materials such as carbon black, acetylene black, ketjen black, channel black, furnace black, lamp black, summer black and carbon fiber; Metal powder or metal fibers such as copper, nickel, aluminum and silver; Conductive whiskey such as zinc oxide and potassium titanate; Conductive metal oxides such as titanium oxide; Or polyphenylene derivatives, and the like, and a single solution or a mixed solution of two or more of them may be used.
  • the conductive material may be included in an amount of 0.1 to 15% by weight based on the total weight of the cathode active material layer.
  • the binder serves to improve the adhesion between the positive electrode active material particles and the adhesion between the positive electrode active material and the current collector.
  • Specific examples include polyvinylidene fluoride (PVDF), vinylidene fluoride-hexafluoropropylene copolymer (PVDF-co-HFP), polyvinylalcohol, polyacrylonitrile, Polypropylene, ethylene-propylene-diene polymer (EPDM), sulphonated-EPDM, polyvinylpyrrolidone, polyvinylpyrrolidone, polyvinylpyrrolidone, Styrene-butadiene rubber (SBR), fluorine rubber, and various copolymers thereof, and one kind or a mixture of two or more kinds of them may be used.
  • the binder may be included in an amount of 0.1 to 15% by weight based on the total weight of the cathode active material layer.
  • the positive electrode may be manufactured according to a conventional positive electrode manufacturing method, except that the positive electrode active material described above is used. Specifically, the cathode active material and optionally the binder and the conductive material may be dissolved or dispersed in a solvent to prepare a composition for forming a cathode active material layer, which is then applied onto the cathode current collector, followed by drying and rolling.
  • the solvent examples include dimethyl sulfoxide (DMSO), isopropyl alcohol, N-methylpyrrolidone (NMP), acetone, and the like. Water and the like, and one kind or a mixture of two or more kinds can be used.
  • the amount of the solvent to be used is sufficient to dissolve or disperse the cathode active material, the conductive material and the binder in consideration of the coating thickness of the slurry and the yield of the slurry, and then to have a viscosity capable of exhibiting excellent thickness uniformity Do.
  • the positive electrode may be produced by casting the composition for forming the positive electrode active material layer on a separate support, and then laminating a film obtained by peeling from the support onto the positive electrode collector.
  • the present invention can produce an electrochemical device including the positive electrode.
  • the electrochemical device may be specifically a battery, a capacitor, or the like, and more specifically, it may be a lithium secondary battery.
  • the lithium secondary battery includes a positive electrode, a negative electrode disposed opposite to the positive electrode, and a separation membrane and an electrolyte interposed between the positive electrode and the negative electrode.
  • the positive electrode is the same as that described above, Only the remaining configuration will be described in detail below.
  • the lithium secondary battery may further include a battery container for housing the electrode assembly of the anode, the cathode, and the separator, and a sealing member for sealing the battery container.
  • the negative electrode includes a negative electrode current collector and a negative electrode active material layer disposed on the negative electrode current collector.
  • the negative electrode current collector is not particularly limited as long as it has high conductivity without causing chemical changes in the battery.
  • the negative electrode current collector may be formed on the surface of copper, stainless steel, aluminum, nickel, titanium, sintered carbon, Carbon, nickel, titanium, silver or the like, aluminum-cadmium alloy, or the like may be used.
  • the negative electrode collector may have a thickness of 3 to 500 ⁇ , and similarly to the positive electrode collector, fine unevenness may be formed on the surface of the collector to enhance the binding force of the negative electrode active material.
  • it can be used in various forms such as a film, a sheet, a foil, a net, a porous body, a foam, and a nonwoven fabric.
  • the anode active material layer optionally includes a binder and a conductive material together with the anode active material.
  • a compound capable of reversible intercalation and deintercalation of lithium may be used.
  • Specific examples thereof include carbonaceous materials such as artificial graphite, natural graphite, graphitized carbon fiber and amorphous carbon;
  • Metal compounds capable of alloying with lithium such as Si, Al, Sn, Pb, Zn, Bi, In, Mg, Ga, Cd, Si alloys, Sn alloys or Al alloys; SiO ⁇ (0 ⁇ ⁇ 2 ), SnO 2, vanadium oxide, which can dope and de-dope a lithium metal oxide such as lithium vanadium oxide;
  • a composite containing the metallic compound and the carbonaceous material such as Si-C composite or Sn-C composite, and any one or a mixture of two or more thereof may be used.
  • a metal lithium thin film may be used as the negative electrode active material.
  • the carbon material may be both low-crystalline carbon and high-crystallinity carbon.
  • Examples of the low-crystalline carbon include soft carbon and hard carbon.
  • Examples of the highly crystalline carbon include natural graphite, artificial graphite, artificial graphite or artificial graphite, Kish graphite graphite, pyrolytic carbon, mesophase pitch based carbon fiber, meso-carbon microbeads, mesophase pitches and petroleum or coal tar coke derived cokes).
  • the negative electrode active material may include 80% by weight to 99% by weight based on the total weight of the negative electrode active material layer.
  • the binder is a component for assisting the bonding between the conductive material, the active material and the current collector, and is usually added in an amount of 0.1% by weight to 10% by weight based on the total weight of the negative electrode active material layer.
  • binders include polyvinylidene fluoride (PVDF), polyvinyl alcohol, carboxymethylcellulose (CMC), starch, hydroxypropylcellulose, regenerated cellulose, polyvinylpyrrolidone, tetrafluoroethylene
  • PVDF polyvinylidene fluoride
  • CMC carboxymethylcellulose
  • EPDM ethylene-propylene-diene polymer
  • sulfonated-EPDM styrene-butadiene rubber
  • fluorine rubber various copolymers thereof.
  • the conductive material may be added in an amount of 10 wt% or less, preferably 5 wt% or less, based on the total weight of the negative electrode active material layer, as a component for further improving the conductivity of the negative electrode active material.
  • a conductive material is not particularly limited as long as it has electrical conductivity without causing chemical changes in the battery, for example, graphite such as natural graphite or artificial graphite; Carbon black such as acetylene black, ketjen black, channel black, furnace black, lamp black, and thermal black; Conductive fibers such as carbon fiber and metal fiber; Metal powders such as carbon fluoride, aluminum, and nickel powder; Conductive whiskey such as zinc oxide and potassium titanate; Conductive metal oxides such as titanium oxide; Conductive materials such as polyphenylene derivatives and the like can be used.
  • the negative electrode active material layer is prepared by applying and drying a composition for forming a negative electrode active material layer, which is prepared by dissolving or dispersing a negative electrode active material on a negative electrode current collector, and optionally a binder and a conductive material in a solvent, Casting a composition for forming an active material layer on a separate support, and then laminating a film obtained by peeling from the support onto a negative electrode current collector.
  • a composition for forming a negative electrode active material layer which is prepared by dissolving or dispersing a negative electrode active material on a negative electrode current collector, and optionally a binder and a conductive material in a solvent, Casting a composition for forming an active material layer on a separate support, and then laminating a film obtained by peeling from the support onto a negative electrode current collector.
  • the negative electrode active material layer may be formed by applying and drying a composition for forming a negative electrode active material layer prepared by dissolving or dispersing a negative electrode active material on a negative electrode collector and optionally a binder and a conductive material in a solvent, Casting the composition on a separate support, and then peeling the support from the support to laminate a film on the negative electrode current collector.
  • the separation membrane separates the cathode and the anode and provides a passage for lithium ion.
  • the separation membrane can be used without any particular limitation as long as it is used as a separation membrane in a lithium secondary battery. Particularly, It is preferable to have a low resistance and an excellent ability to impregnate the electrolyte.
  • porous polymer films such as porous polymer films made of polyolefin-based polymers such as ethylene homopolymers, propylene homopolymers, ethylene / butene copolymers, ethylene / hexene copolymers and ethylene / methacrylate copolymers, May be used.
  • a nonwoven fabric made of a conventional porous nonwoven fabric for example, glass fiber of high melting point, polyethylene terephthalate fiber, or the like may be used.
  • a coated separator containing a ceramic component or a polymer material may be used, and the separator may be selectively used as a single layer or a multilayer structure.
  • Examples of the electrolyte used in the present invention include an organic liquid electrolyte, an inorganic liquid electrolyte, a solid polymer electrolyte, a gel-type polymer electrolyte, a solid inorganic electrolyte, and a molten inorganic electrolyte that can be used in the production of a lithium secondary battery. It is not.
  • the electrolyte may include an organic solvent and a lithium salt.
  • the organic solvent may be used without limitation as long as it can act as a medium through which ions involved in the electrochemical reaction of the battery can move.
  • examples of the organic solvent include ester solvents such as methyl acetate, ethyl acetate,? -Butyrolactone and?
  • Ether solvents such as dibutyl ether or tetrahydrofuran; Ketone solvents such as cyclohexanone; Aromatic hydrocarbon solvents such as benzene and fluorobenzene; Dimethyl carbonate (DMC), diethylcarbonate (DEC), methylethylcarbonate (MEC), ethylmethylcarbonate (EMC), ethylene carbonate (EC), propylene carbonate PC) and the like; Alcohol solvents such as ethyl alcohol and isopropyl alcohol; R-CN (R is a linear, branched or cyclic hydrocarbon group having 2 to 20 carbon atoms, which may contain a double bond aromatic ring or an ether bond); Amides such as dimethylformamide; Dioxolanes such as 1,3-dioxolane; Or sulfolane may be used.
  • Ether solvents such as dibutyl ether or tetrahydrofuran
  • Ketone solvents such as cyclohex
  • a carbonate-based solvent is preferable, and a cyclic carbonate (for example, ethylene carbonate or propylene carbonate) having a high ionic conductivity and a high dielectric constant, for example, such as ethylene carbonate or propylene carbonate, For example, ethyl methyl carbonate, dimethyl carbonate or diethyl carbonate) is more preferable.
  • a cyclic carbonate for example, ethylene carbonate or propylene carbonate
  • ethylene carbonate or propylene carbonate for example, ethylene carbonate or propylene carbonate
  • ethyl methyl carbonate, dimethyl carbonate or diethyl carbonate ethyl methyl carbonate, dimethyl carbonate or diethyl carbonate
  • the lithium salt can be used without particular limitation as long as it is a compound capable of providing lithium ions used in a lithium secondary battery.
  • the lithium salt LiPF 6, LiClO 4, LiAsF 6, LiBF 4, LiSbF 6, LiAl0 4, LiAlCl 4, LiCF 3 SO 3, LiC 4 F 9 SO 3, LiN (C 2 F 5 SO 3) 2 , LiN (C 2 F 5 SO 2) 2, LiN (CF 3 SO 2) 2.
  • LiCl, LiI, or LiB (C 2 O 4 ) 2 may be used.
  • the concentration of the lithium salt is preferably in the range of 0.1 to 2.0 M. When the concentration of the lithium salt is within the above range, the electrolyte has an appropriate conductivity and viscosity, so that it can exhibit excellent electrolyte performance and the lithium ion can effectively move.
  • the electrolyte may contain, for example, a haloalkylene carbonate-based compound such as difluoroethylene carbonate or the like, pyridine, triethanolamine, or the like for the purpose of improving lifetime characteristics of the battery, Ethyl phosphite, triethanol amine, cyclic ether, ethylenediamine, glyme, hexametriamide, nitrobenzene derivatives, sulfur, quinone imine dyes, N-substituted oxazolidinones, N, At least one additive such as benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, benzyl alcohol, The additive may be included in an amount of 0.1 to 5% by weight based on the total weight of the electrolyte.
  • the lithium secondary battery including the cathode active material according to the present invention stably exhibits excellent discharge capacity, output characteristics and life characteristics, it can be used in portable devices such as mobile phones, notebook computers, digital cameras, and hybrid electric vehicles hybrid electric vehicle (HEV)).
  • portable devices such as mobile phones, notebook computers, digital cameras, and hybrid electric vehicles hybrid electric vehicle (HEV)).
  • HEV hybrid electric vehicles hybrid electric vehicle
  • a battery module including the lithium secondary battery as a unit cell and a battery pack including the same.
  • the battery module or the battery pack may include a power tool; An electric vehicle including an electric vehicle (EV), a hybrid electric vehicle, and a plug-in hybrid electric vehicle (PHEV); Or a power storage system, as shown in FIG.
  • a power tool including an electric vehicle (EV), a hybrid electric vehicle, and a plug-in hybrid electric vehicle (PHEV); Or a power storage system, as shown in FIG.
  • EV electric vehicle
  • PHEV plug-in hybrid electric vehicle
  • the external shape of the lithium secondary battery of the present invention is not particularly limited, but may be a cylindrical shape, a square shape, a pouch shape, a coin shape, or the like using a can.
  • the lithium secondary battery according to the present invention can be used not only in a battery cell used as a power source of a small device but also as a unit cell in a middle- or large-sized battery module including a plurality of battery cells.
  • LiNi 0 . 8 Co 0 . 1 Mn 0 . 1 Zr 0 . 04 S 0 . 03 O 2 was mixed with 100 mL of H 3 BO 3 of pH 6 and reacted for 1 hour to form Li 3 BO 3 on the surface. This was dried at 150 ° C and then heat-treated at 300 ° C to prepare a cathode active material having a Li-BO compound layer containing Li 3 BO 3 and LiBO 2 on the surface and having a thickness of 10 nm.
  • the cathode active material: carbon black conductive material: PVdF binder prepared above was mixed in a weight ratio of 95: 2.5: 2.5 in N-methylpyrrolidone solvent to prepare a composition for forming a positive electrode. This was coated on an Al current collector having a thickness of 20 mu m, followed by drying and roll pressing to produce a positive electrode.
  • lithium metal was used as a counter electrode.
  • the prepared positive electrode and lithium metal were laminated together with a Celgard 2300 separator (Celgard) to prepare an electrode assembly.
  • the electrode assembly was placed in a battery case, and ethylene carbonate (EC): ethyl methyl carbonate (EMC): diethyl carbonate ) was mixed at a volume ratio of 40:30:30, and 1 M of LiPF 6 was dissolved in the mixed solvent to prepare a lithium secondary battery.
  • EC ethylene carbonate
  • EMC ethyl methyl carbonate
  • LiPF 6 diethyl carbonate
  • LiNi 0 . 8 Co 0 . 1 Mn 0 . 1 Zr 0 . 04 S 0 . 03 O 2 was mixed with 100 mL of H 3 PO 4 of pH 3 and reacted for 1 hour to prepare a cathode active material having a Li 3 PO 4 layer on the surface thereof.
  • a positive electrode and a lithium secondary battery including the positive electrode were prepared.
  • a cathode active material in which a Li-BO compound containing LiBO 2 and Li 2 B 4 O 7 was non-uniformly formed on the surface of O 2 was prepared.
  • a positive electrode and a lithium secondary battery including the positive electrode were prepared in the same manner as in Example 1, except that the prepared positive electrode active material was used.
  • a positive electrode and a lithium secondary battery including the positive electrode were prepared in the same manner as in Example 1 except that 1 O 2 was used as the positive electrode active material.
  • Example 1 and Comparative Example 1 were each charged at a constant current of 1 C at 25 ⁇ to a voltage of 4.4 V at a cut off of 0.05 C. Thereafter, discharge was performed until the voltage reached 3 V with a constant current of 1C.
  • the charging and discharging behaviors were set as one cycle. After repeating this cycle 100 times, the capacity retention and the rate of increase in resistance of the lithium secondary battery according to Example 1 and Comparative Example 1 were measured.
  • the life characteristics and resistance characteristics of Example 1 and Comparative Example 1 measured in Experimental Example 1 are shown in Fig. 1 and Table 1 below.
  • the resistances of the lithium secondary batteries manufactured in Examples 1 and 2 in the 100th cycle were 74? And 78?, Respectively.
  • the initial resistance of the lithium secondary battery manufactured in Examples 1 and 2 was 25 ⁇ , which was 2.9% and 3.1% after 100 cycles, respectively.
  • the initial resistance of the lithium secondary battery manufactured in Comparative Examples 1 to 4 was about 20 ⁇ , and the resistance increase rate after 100 cycles was about 4% to 7.3%, which indicates a much larger resistance increase rate than the present invention I could.
  • resistance characteristics were further improved by forming a uniform coating layer on the surface.

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JP7137602B2 (ja) 2020-09-18 2022-09-14 プライムプラネットエナジー＆ソリューションズ株式会社 被膜付き正極活物質粒子の製造方法

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